A clinical trial to assess the confidence, usability, preference and satisfaction on use of Dry Powder Inhaler (DPI) in healthy volunteers and in subjects with mild asthma or COPD.
Phase 4
Completed
- Conditions
- Health Condition 1: null- Healthy Volunteers and in subjects with mild Asthma or COPD
- Registration Number
- CTRI/2009/091/000215
- Lead Sponsor
- Cipla Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
1. Subjects and healthy volunteers willing to sign informed consent
2. Subjects and healthy volunteers of 18 years and above
3. Subjects with or without a respiratory condition. Each subject with a respiratory condition (prior experience of using an inhaler) should be matched as far as possible with an individual without a respiratory condition (inhaler naïve) with respect to the age, sex, literacy status etc
4. Subjects with mild Asthma or COPD
Exclusion Criteria
1. Subjects already using Dry Powder Inhaler (DPI) prior to start of the study.
2. Subjects with co-ordination problems like Parkinson?s disease, mental illness, tremors etc.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method